Infraorbital / upper and lower eyelids

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16 Infraorbital / upper and lower eyelids

Anatomy of the eye

Complete knowledge and understanding of both dynamic and volumetric changes in the face, as well as the interaction between and function of various facial musculature and the surrounding soft tissue, are critical to ensuring successful outcomes with the use of BoNT in the periorbital region. Although in-depth examinations of facial anatomy have been published elsewhere, this chapter focuses on the anatomy of the eye relevant to the use of BoNT in the upper and lower eyelids (Fig. 16.1).

The upper eyelid extends from the eyelid margin to the eyebrow superiorly, with the superior palpebral sulcus (associated with the upper eyelid skin crease) located lengthwise between the medial canthus and the lateral orbital rim, approximately in the range of 8–11 mm superior to the eyelid margin. The lower eyelid extends below the inferior orbital rim to join the cheek. In youth, the inferior palpebral sulcus (lower eyelid fold) is located 3–5 mm from the lower lid margin.

The orbicularis oculi – the sphincter muscle of the eyelids – is a wide, concentric band of muscle comprising the palpebral component, which can be further divided into pretarsal and preseptal portions and is responsible for blinking and gentle eyelid closure, and the orbital component, responsible for forceful lid closure and the production of lateral canthal and lower eyelid rhytides. Superiorly, the orbital component interdigitates with other superficial muscles of facial expression, including the frontalis, corrugator, and the depressor supercilii muscles, laterally it comes into proximity of the overlying fascia of the temporalis muscles, and the muscles of the inferior quadratus labii superioris and zygomaticus complex. Inferiorly, the orbicularis lies flat across the cheek and is considered a part of the superficial musculoaponeurotic system (SMAS), which translates muscle movement into movement of the skin. At the junction of the lower lid with the cheek, the orbicularis oculi muscle forms a direct attachment with the orbital rim at the junction of the palpebral and orbital portions.

Patient assessment and selection

Because successful use of BoNT in the periorbital region demands close attention to anatomical variations and individualized treatment, a thorough evaluation of every patient is mandatory. Comprehensive assessment will include patient education and counseling, medical history, and physical examination of the periorbital region and area to be treated.

Communication between patient and clinician builds trust and ensures that expectations do not exceed realistic outcomes. Evaluation of periorbital concerns in discussion as well as physical examination will avoid post-injection problems. Interviews should address the patient’s current ophthalmic status including the presence of dry eye symptoms as well as the transient nature of BoNT injections, the need for frequent touch-ups, common injection-related side effects, and potential complications. Informed consent is essential.

A complete medical and ophthalmic history is necessary, including previous experiences with rejuvenation procedures, surgery, and any other conditions that might influence treatment plans or outcome. The degree of rhytides and their potential response to treatment can be assessed via the Glogau photoaging scale (Table 16.1). Moreover, the quality of skin around the eye will also determine a treatment plan: patients with excessive skin above the eye, prominent fat pads in the lower lid, septal fat herniation, or severe elastosis (identified by a positive snap test), may require additional rejuvenating procedures such as laser or light-based therapies or even surgery prior to augmentation. All findings (including any sign of ptosis or asymmetry) should be noted and discussed with the patient, and standard digital photographs taken both before and after any treatments. Photographs should display the face in repose and at maximal expression to document changes on animation.

Table 16.1 Wrinkle severity and rejuvenation requirements

Group severity* Description Rejuvenation modalities
II Moderate; wrinkles in motion Responds well to BoNT alone
III Advanced; wrinkles at rest BoNT plus additional correction, such as soft tissue augmentation
IV Severe; only wrinkles BoNT plus deeper skin resurfacing for maximal improvement

* Based on the Glogau classification of photoaging.

Not everyone is a candidate for BoNT therapy. Aside from general contraindications (Box 16.1), caution should prevail in patients with a history and especially complications related to previous lower eyelid blepharoplasty and injections avoided in patients with lower lid laxity, due to the risk of scleral show, pre-existing conditions that could be worsened by treatment, such as mid-facial paresis or symptomatic dry eyes, stable or progressive muscular dystrophic conditions causing blepharoptosis, or anyone with already-compromised function of the orbicularis oculi.

Indications and techniques

Consensus recommendations have been developed for dosing and techniques in all areas of the face, although treatment must be individualized according to muscle size and function and desired outcome. In the upper and lower lid, precise placement of injections and conservative doses are crucial in avoiding adverse effects and obtaining the most beneficial effects.

Hypertrophic orbicularis, infraorbital rhytides, and widening of the eye

Infraorbital rhytides radiating below the eyes toward the cheek arise from concentric contraction of the orbicularis oculi peripheral to the lines. Moreover, such hypertrophy of the pretarsal portion of the orbicularis oculi contributes to the perception of lower eyelid bags (a ‘jelly roll’ appearance) and a narrowing of the palpebral aperture, particularly when the patient smiles. A series of studies conducted by Flynn & Carruthers have shown that 2 U BoNT placed subdermally in the lower eyelid in the midpupillary line, 3 mm below the ciliary margin (Fig. 16.2) can relax and flatten the pretarsal orbicularis, improving the appearance of the lower lid. Similar injections in the lower lid with concomitant treatment of the lateral canthal rhytides (three injections of 4 U each, for a total of 12 U) can produce increases of approximately 2–3 mm in the vertical palpebral aperture at rest and full smile, respectively, giving the lower eyelid a more rounded appearance (Fig. 16.3). Further examination by Flynn & Carruthers demonstrated a clear dose response when the lower lid was treated alone; however, higher doses led to an increase in side effects and did not further enhance the size of the palpebral aperture. The authors therefore recommend a conservative approach with the smallest dose (1–2 U at two sites) in the lower lid, with retreatment after 2–4 weeks if necessary.

Case Study 1 (see Fig. 16.2)

A healthy 32-year-old Filipino-Canadian woman presented complaining of a ‘jelly roll’ underneath her eyes when she smiled. She requested a more western wide-eyed look and reduction of the ‘jelly roll’. Figure 16.2A demonstrates a hypertrophic orbicularis oculi. A ‘snap-test’ demonstrated excellent elasticity, which, in conjunction with the youthful tone and texture of the skin, indicated that the patient was a suitable candidate for infraorbital BoNT-A treatment. In order to achieve a wider aperture and flattening of hypertrophic orbicularis oculi (Fig. 16.2B) 2 U of BoNT-A were injected in the mid-pupillary line 4 mm below the lid margin bilaterally. Figure 16.2C demonstrates the injection site and technique.

Lid ptosis, malposition, and asymmetry

BoNT is an effective treatment for the temporary management of mild-to-moderate upper lid ptosis, malposition, and eyelid-fissure asymmetry. Research by Fagien indicates that correct placement, dosing, and careful patient selection will determine predictability of response. Typically, eyelid malposition of any etiology has been treated by surgical correction of the underlying cause, with nonsurgical options for upper lid ptosis limited to adrenergic topical ophthalmic drops. Low-dose subdermal injection of BoNT (0.5–1.5 U) into the extreme medial and lateral aspects of the pretarsal region of the orbicularis just above the lash line (Figs 16.4 and 16.5) allows unopposed activity of the levator palpebrae and Müller’s muscle, and a return to symmetry.

Likewise, lower lid asymmetry and malposition (such as retraction, ectropion, and entropion) have historically been treated with surgical intervention to tighten or shorten the horizontal length of the lower eyelid to achieve symmetry with the contralateral side. Malposition and symmetry can be restored to the lower eyelid by weakening the lower lid elevators on the side opposite the lower lid retractions by two injections of BoNT: one placed at the extreme lateral aspect of the lower eyelid, the other at the mid aspect of the lower eyelid pretarsal region, located approximately mid-pupil, inducing a similar, retracted effect.

Doses in the upper and lower lids range from 0.5 to 1.5 U per injection site, with higher doses reserved for cases of lower eyelid hypertrophy and severe ptosis, or when changing the position of the lower eye.

Adjunctive treatments for the lid

Increasingly, each aspect of facial rejuvenation is viewed as a whole, using combination therapies to provide the best possible outcomes. There are a variety of treatments aimed at improving the appearance of the eye that can be used in combination with BoNT for a synergistic effect, targeting not only improvement in rhytides but also in pigmentation, texture, scarring, and laxity.

Adverse events

Bruising and ecchymosis are the most common injection-site reactions to BoNT in the periorbital area. The addition of sublingual Arnica montana immediately following and then four times a day for 2–3 days may minimize bruising, as will superficial injections and the application of ice immediately following treatment.

More serious adverse effects can occur, usually due to inappropriate dosing or injection technique (Table 16.2). Some patients describe a temporary feeling of ‘fullness’ in the lower lid following treatment. In rare cases, but particularly in patients with excessive lower lid laxity, this may manifest as edema that is worse in the morning. It is believed that this results from inactivity of the orbicularis oculi, which aids in the drainage of lymphatic fluid. Rare complications in the periocular area include lower eyelid laxity, scleral show, epiphora, ectropion, diplopia, dry eye, incomplete eyelid closure, and ptosis. Careful patient selection and attention to anatomical features of the periorbital region can aid in avoiding most of these side effects, all of which eventually disappear over time due to the transient effect of BoNT. Goldman reported a case of prominent festoon formation after 2 U 2–3 mm below the ciliary margin in the mid-pupillary line and 10 U (single injection) in the mid-lateral canthal region. Only at the follow-up visit did the patient admit to a previous facelift, forehead lift, and lower eyelid blepharoplasty 8 years previously. This case scenario emphasizes the importance of pre-treatment history and physical examination of the lower eyelid structure and function before treatment with even small doses of BoNT. Upper eyelid complications can also be avoided by careful thought, injection technique, and placement. Mild lagophthalmos can be induced in the upper eyelid by greater than necessary dosages and can generally be avoided with doses less than 1.5 U. This too, stresses the need for an initial conservative approach that can be titrated to the most effective dose.

Table 16.2 Injection-related complications

Cause Complication
Treatment of lower lid pretarsal orbicularis in patients with severe elastosis and retraction Ectropion, scleral show; accentuation of drooping or rhytides in lower lid; lower lid fat herniation
Diffusion of toxin behind orbital septum Eyelid Ptosis
Injections near trochlea in upper or lower eyelid Diplopia
Paralysis of orbicularis oculi Epiphora; ectropion

Administering injections peripheral to the orbital rim and using a higher concentration and smaller volume may also avoid infiltration of the toxin into the vicinity of the extraocular muscles. Avoiding the pretarsal region (and choosing the lateral preseptal area) for the treatment of lower lid rhytides will both improve the aesthetic effect and decrease the likelihood of functional adverse effects and malposition.

Further reading

Balikian RV, Zimbler MS. Primary and adjunctive uses of botulinum toxin type A in the periorbital region. Otolaryngology Clinics of North America. 2007;40:291–303.

Carruthers J, Carruthers A. Adjunctive botulinum toxin type A: fillers and light-based therapies. International Ophthalmology Clinics. 2005;45:143–151.

Carruthers J, Fagien S, Matarasso SL, Botox Consensus Group. Consensus recommendations on the use of botulinum toxin type a in facial aesthetics. Plastic Reconstructive Surgery. 2004;114(6 suppl):S1–S22.

Cohen JL. Enhancing the growth of natural eyelashes: the mechanism of bimatoprost-induced eyelash growth. Dermatologic Surgery. 2010;36:1361–1371.

Fagien S. Botox for the treatment of dynamic and hyperkinetic facial lines and furrows: adjunctive use in facial aesthetic surgery. Plastic Reconstructive Surgery. 1999;103:701–713.

Fagien S. Botulinum toxin type A for facial aesthetic enhancement: role in facial shaping. Plastic and Reconstructive Surgery. 2003;112(5 suppl):S6–S18.

Fagien S. Temporary management of upper lid ptosis, lid malposition, and eyelid fissure asymmetry with botulinum toxin type A. Plastic and Reconstructive Surgery. 2004;114:1892–1902.

Fagien S, Brandt FS. Primary and adjunctive use of botulinum toxin type A (Botox) in facial aesthetic surgery: beyond the glabella. Clinics in Plastic Surgery. 2001;28:127–148.

Fagien S, Raspaldo H. Facial rejuvenation with botulinum neurotoxin: an anatomical and experiential perspective. Journal of Cosmetic and Laser Therapy. 2007;9(suppl 1):23–31.

Fagien S. Management of hypotrichosis of the eyelashes: Focus on bimatoprost. Cosmetic, Clinical, and Investigational Dermatology. 2010;3:1–10.

Flynn TC. Periocular botulinum toxin. Clinics in Dermatology. 2003;21:498–504.

Flynn TC, Carruthers JA, Carruthers JA. Botulinum-A toxin treatment of the lower eyelid improves infraorbital rhytides and widens the eye. Dermatologic Surgery. 2001;27:703–708.

Flynn TC, Carruthers JA, Carruthers JA, et al. Botulinum A toxin (BOTOX) in the lower eyelid: dose-finding study. Dermatologic Surgery. 2003;29:943–950.

Glaser DA, Patel U. Enhancing the eyes: use of minimally invasive techniques for periorbital rejuvenation. Journal of Drugs in Dermatology. 2010;9:S118–S128.

Glavas IP, Purewal BK. Noninvasive techniques in periorbital rejuvenation. Facial Plastic Surgery. 2007;23:162–167.

Glogau RG. Aesthetic and anatomic analysis of the aging skin. Seminars in Cutaneous Medicine and Surgery. 1996;15:134–138.

Goldman MP. Festoon formation after infraorbital botulinum A toxin: a case report. Dermatologic Surgery. 2003;29:560–561.

Harris PA, Mendelson BC. Eyelid and midcheek anatomy. In: Fagien S, ed. Putterman’s Cosmetic Ocuplasticsurgery. 4th edn. Philadelphia: WB Saunders; 2007:45–63.

Matarasso SL, Matarasso A. ‘M’ marks the spot: update on treatment guidelines for botulinum toxin type A for the periocular area. Plastics and Reconstructive Surgery. 2003;112:1470–1472.

Smith S, Fagien S, Whitcup S, et al. Eyelash growth in subjects treated with bimatoprost: A multicenter, randomized, double-masked, vehicle-controlled, parallel group study. Journal of the American Academy of Dermatology. 2011. Sep 5 [Epub ahead of print]